ENST00000267845.8:c.1724T>G
MANE Select
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ENSP00000267845.3:p.Val575Gly
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ENST00000267845.7:c.1724T>G
|
ENSP00000267845.3:p.Val575Gly
|
|
ENST00000543581.5:c.1625T>G
|
ENSP00000440252.1:p.Val542Gly
|
|
ENST00000559816.1:n.1468T>G
|
|
|
NM_001306146.1:c.1625T>G
|
NP_001293075.1:p.Val542Gly
|
|
NM_002112.3:c.1724T>G
|
NP_002103.2:p.Val575Gly
|
|
XM_011521479.1:c.1487T>G
|
XP_011519781.1:p.Val496Gly
|
|
XM_011521480.1:c.1292T>G
|
XP_011519782.1:p.Val431Gly
|
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XM_017022094.1:c.1829T>G
|
XP_016877583.1:p.Val610Gly
|
|
XM_017022095.1:c.1730T>G
|
XP_016877584.1:p.Val577Gly
|
|
XM_017022096.1:c.1601T>G
|
XP_016877585.1:p.Val534Gly
|
|
XM_017022097.1:c.1592T>G
|
XP_016877586.1:p.Val531Gly
|
|
XM_017022098.1:c.1397T>G
|
XP_016877587.1:p.Val466Gly
|
|
NM_002112.4:c.1724T>G
MANE Select
|
NP_002103.2:p.Val575Gly
|
|
NM_001306146.2:c.1625T>G
|
NP_001293075.1:p.Val542Gly
|
|